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一种检测和缓解还原性应激的细胞机制。

A Cellular Mechanism to Detect and Alleviate Reductive Stress.

机构信息

Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley CA 94720, USA.

Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley CA 94720, USA; Howard Hughes Medical Institute, University of California at Berkeley, Berkeley CA 94720, USA.

出版信息

Cell. 2020 Oct 1;183(1):46-61.e21. doi: 10.1016/j.cell.2020.08.034. Epub 2020 Sep 16.

Abstract

Metazoan organisms rely on conserved stress response pathways to alleviate adverse conditions and preserve cellular integrity. Stress responses are particularly important in stem cells that provide lifetime support for tissue formation and repair, but how these protective systems are integrated into developmental programs is poorly understood. Here we used myoblast differentiation to identify the E3 ligase CUL2 and its substrate FNIP1 as core components of the reductive stress response. Reductive stress, as caused by prolonged antioxidant signaling or mitochondrial inactivity, reverts the oxidation of invariant Cys residues in FNIP1 and allows CUL2 to recognize its target. The ensuing proteasomal degradation of FNIP1 restores mitochondrial activity to preserve redox homeostasis and stem cell integrity. The reductive stress response is therefore built around a ubiquitin-dependent rheostat that tunes mitochondrial activity to redox needs and implicates metabolic control in coordination of stress and developmental signaling.

摘要

后生动物依靠保守的应激反应途径来减轻不利条件并维持细胞完整性。应激反应在后生动物干细胞中尤为重要,这些干细胞为组织形成和修复提供终身支持,但这些保护系统如何整合到发育程序中还知之甚少。在这里,我们利用成肌细胞分化来鉴定 E3 连接酶 CUL2 及其底物 FNIP1 作为还原应激反应的核心组成部分。还原应激,如由抗氧化信号的延长或线粒体失活引起的,会使 FNIP1 中不变的半胱氨酸残基的氧化还原,并使 CUL2 能够识别其靶标。随后 FNIP1 的蛋白酶体降解恢复线粒体活性,以维持氧化还原平衡和干细胞完整性。因此,还原应激反应是围绕一个依赖于泛素的变阻器构建的,该变阻器调节线粒体活性以适应氧化还原需求,并暗示代谢控制在协调应激和发育信号方面的作用。

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